| Literature DB >> 33319463 |
Maritess Arancillo1, Jaru Taechalertpaisarn1, Xiaowen Liang2, Kevin Burgess1.
Abstract
Small molecule probe development is pivotal in biomolecular science. Research described here was undertaken to develop a non-peptidic chemotype, piptides, that is amenable to convenient, iterative solid-phase syntheses, and useful in biomolecular probe discovery. Piptides can be made from readily accessible pip acid building blocks and have good proteolytic and pH stabilities. An illustrative application of piptides against a protein-protein interaction (PPI) target was explored. The Exploring Key Orientations (EKO) strategy was used to evaluate piptide candidates for this. A library of only 14 piptides contained five members that disrupted epidermal growth factor (EGF) and its receptor, EGFR, at low micromolar concentrations. These piptides also caused apoptotic cell death, and antagonized EGF-induced phosphorylation of intracellular tyrosine residues in EGFR.Entities:
Keywords: EGF; cancer; peptidomimetics; protein-protein interactions; solid-phase synthesis
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Year: 2021 PMID: 33319463 PMCID: PMC7940574 DOI: 10.1002/anie.202015203
Source DB: PubMed Journal: Angew Chem Int Ed Engl ISSN: 1433-7851 Impact factor: 15.336